Evidence map›Paper›PMID 16840331›Full record

ArticleJournal of virology2006

Mouse cytomegalovirus crosses the species barrier with help from a few human cytomegalovirus proteins.

Qiyi Tang, Gerd G Maul

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Decoding murine cytomegalovirus.PLoS pathogens · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
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  13. Article
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  16. Review
  17. Article
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  19. UL36 Rescues Apoptosis Inhibition andFrontiers in cellular and infection microbiology · 2017
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Qiyi TangThe Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA.
Gerd G Maul
The Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
EARLY INTERACTIONS OF DNA VIRUSES AND HOSTR01AI041136 · NIAID · WISTAR INSTITUTE · PI MAUL, GERD G · 1998 to 2005
$1.8M
Early interactions of DNA viruses and hostR56AI041136 · NIAID · WISTAR INSTITUTE · PI KAUFMAN, RUSSEL E. · 2008 to 2009
$828k
EARLY INTERACTIONS OF DNA VIRUSES AND HOSTR21AI041136 · NIAID · WISTAR INSTITUTE · PI MAUL, GERD G · 1997 to 1997
–
VIRUS DNA TARGETING MECHANISM--THE TARGETR21GM057599 · NIGMS · WISTAR INSTITUTE · PI MAUL, GERD G · 1998 to 1999
–
NCI NIH HHS CA 10815NCI NIH HHS P30 CA010815NIAID NIH HHS AI 41136NIAID NIH HHS R01 AI041136NIAID NIH HHS R56 AI041136NIGMS NIH HHS GM 57599
6 · The paper itself

Abstract

Strong species specificity and similar tropisms suggest mouse cytomegalovirus (mCMV) as a potential vector for transgenes into human cells. We reexamined the dogma that mouse cytomegalovirus cannot productively replicate in human cells and found that mouse cytomegalovirus can produce infectious particles albeit at a level that does not sustain an infection. This finding demonstrates that mouse cytomegalovirus can undergo all processes of its life cycle in human cells but may not be well adapted to circumvent the human cell's intrinsic defenses. The suppression of mCMV production in human cells is affected at several levels, which additively or synergistically result in the appearance of species specificity. Hydrolysis of most newly replicated viral DNA and very low capsid protein transcription reduced the potential particle production to insignificant levels. These effects can be ameliorated by adding human cytomegalovirus tegument proteins and immediate-early protein 1. They function synergistically to produce significant amounts of mCMV in human cells. While the possibility that mouse cytomegalovirus might replicate in human cells raises caution in the use of this virus as a transgene vector, manipulation of the mouse cytomegalovirus genome to allow limited spread to other human cells might also provide an advantage for the distribution of certain transgenic products.

Indexed as

DNA ReplicationAnimalsCapsid ProteinsDNA, ViralFibroblastsHeLa CellsHerpesviridae InfectionsHumansImmediate-Early ProteinsImmunoblottingIn Situ Hybridization, FluorescenceMiceMuromegalovirusNIH 3T3 CellsReverse Transcriptase Polymerase Chain ReactionSkinCapsid ProteinsDNA, ViralIE1 protein, cytomegalovirusImmediate-Early ProteinsViral Proteins

Identifiers

PMID16840331
PMCPMC1563706
OpenAlexW2140807899

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.